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Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application
Sponsor: W.L.Gore & Associates
Summary
The SYN 20-01 Study is a non-interventional, prospective, multicenter, multicohort, international, post-market clinical investigation looking into the assessment of GORE® SYNECOR Biomaterial in focused patient populations and in long-term application. Patients with ventral / incisional hernia amenable to hernia mesh repair will be enrolled into two cohorts (US and EU cohort) and followed-up over the period of 60 months.
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
OBSERVATIONAL
Enrollment
320
Start Date
2023-02-24
Completion Date
2030-07-31
Last Updated
2026-01-21
Healthy Volunteers
No
Interventions
Hernia repair with mesh
Hernia repair with GORE® SYNECOR Biomaterial; technical approach laparoscopic, robotic or open surgical / minimally invasive surgery
Locations (15)
Emory Saint Joseph's Hospital
Atlanta, Georgia, United States
Tufts Medical Center
Boston, Massachusetts, United States
Corewell Health
Grand Rapids, Michigan, United States
Lovelace Women's Hospital
Albuquerque, New Mexico, United States
Stony Brook University Hospital
Stony Brook, New York, United States
Novant Health New Hanover Regional Medical Center
Wilmington, North Carolina, United States
Prisma Health Greenville Memorial Hospital
Greenville, South Carolina, United States
Bon Secours Memorial Regional Medical Center
Mechanicsville, Virginia, United States
Ospedale Civile di Baggiovara
Baggiovara, Italy
Vincenzo Monaldi Hospital
Naples, Italy
Sapienza Università di Roma
Roma, Italy
University Hospital Virgen Macarena - Department of General And Digestive Surgery
Seville, Spain
Hospital Quirón Salud-Sagrado Corazón
Seville, Spain
University Hospitals Birmingham NHS Foundation Trust - Queen Elizabeth Hospital Birmingham
Birmingham, United Kingdom
Walsall Manor Hospital
Walsall, United Kingdom